Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1176354329
Device Listing 1176354329
Listing Summary
#
Listing key
1176354329
Premarket submission
K871802
Device
MODEL K210 AND K211 FLUIDOTHERAPY UNITS
Applicant
Henley Intl.
Product code
LSB
Decision date
1987-09-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
15614
9616086
3006076154
Dave Hunter
1
N
2026-01-01
5919 Sea Otter Place Suite 200 Carlsbad CA US 92010